PuriActives® S-Glucan

PuriActives® S-Glucan

Sulfated polysaccharide technology for sensitive and stressed skin

01 · THE FORMULATION CHALLENGE · THE CHALLENGE

Efficacy keeps advancing — tolerability has not kept up

High-efficacy actives — retinoids, exfoliating acids, vitamin C — remain the strongest drivers of visible skincare results, and are also among the most common triggers of stinging, visible redness and barrier stress. For a growing number of consumers, the bottleneck of a skincare routine is no longer efficacy, but how much stress the skin can withstand.

Everyday stress scenarios that amplify skin reactivity

● Retinoid adjustment periods and over-exfoliation

● Acid peels and high-strength vitamin C routines

● UV, pollution and climate-change stress

● Aesthetic procedures — laser, peels, microneedling

● Shaving and daily mechanical friction

60–70%of women self-report some degree of sensitive skin; 50–60% of men do as wellFarage MA, Cosmetics, 2019 44.6%of American adults self-report “sensitive” or “very sensitive” skin in a representative national surveyMisery L et al., Int J Dermatol, 2011

Formulation insight: every high-efficacy system now needs a built-in tolerability strategy — starting at the ingredient level.

02 · MARKET CONTEXT · THE MARKET

Sensitive skin & barrier repair: a structural growth engine

$80.3BDermocosmetic skincare market size in 2031, up from $50.3B in 2025 — an 8.1% CAGR; dermatology-backed skincare is going mainstreamMordor Intelligence, 2026 edition +9.9%Forecast CAGR of the sensitive-skin segment (2026–2031) — the fastest-growing skin-need trackMordor Intelligence, 2026 edition $12.6BRepairing skincare market size in 2036, growing from $6.9B in 2026, driven by post-procedure and post-retinoid care demandFuture Market Insights, 2026

The formulation trends behind the numbers

Barrier-first skincare · post-procedure and post-laser repair · “skinimalism” — fewer, better-validated ingredients

Recovery after retinoids and acids · skin resilience as a claim territory · dermatologist-channel daily care

The opportunity: advanced soothing and repair actives are no longer a niche add-on — they are becoming shared formulation infrastructure for sensitive-skin and high-efficacy products alike.

03 · INGREDIENT INTRODUCTION · THE INGREDIENT

Meet PuriActives® S-Glucan

“Answering skin repair with a sulfated polysaccharide.”

PuriActives® S-Glucan is a low-molecular-weight sulfated polysaccharide — the sodium salt of sulfated dextran — developed for modern soothing, anti-redness, barrier-support and post-stress repair formulations.

Sulfating the dextran backbone converts a neutral, passive polysaccharide into a strong polyanionic macromolecule, fundamentally changing its interaction profile: high negative charge density, strong water binding, protective-film formation, and electrostatic interactions with positively charged proteins and inflammatory mediators.

The result is an ingredient category of its own — not a renamed β-glucan, but a next-generation repair active with published evidence across inflammatory, vascular and sensitive-skin models.

INCI name Sodium Dextran Sulfate
CAS No. 9011-18-1
Molecular weight 9–20 kDa standard grade · 4–8 kDa grade
Appearance White to off-white powder
Solubility Readily soluble in water
Recommended use level 0.05–0.20%

04 · CATEGORY DEFINITION · THE CATEGORY

S-Glucan is not “just another glucan”

What sulfation changes: it converts a passive hydrating polysaccharide into an interactive, bioactive polyanion — a different chemical and functional category, not a line extension of β-glucan.

05 · SCIENTIFIC IDENTITY · THE SCIENCE

From dextran to sodium dextran sulfate

01 · The backbone

Dextran is a fermentation-derived branched glucose polymer dominated by α-1,6 glycosidic linkages — a neutral, uncharged polysaccharide.

02 · The chemical modification

Sulfation replaces backbone –OH groups with sulfate ester groups (–O–SO₃⁻ Na⁺), yielding a strongly anionic polymer with high charge density.

03 · The functional outcome

The polyanion binds water, forms a hydrating surface film, and interacts electrostatically with cationic proteins and inflammatory mediators.

06 · WHY CHARGE MATTERS · WHY CHARGE MATTERS

A polyanionic structure built for biological interaction

Electrostatic interaction. The dense sulfate charges interact with positively charged proteins and signaling mediators — including those that drive inflammatory amplification at the skin surface.

Glycosaminoglycan-like properties. Sulfated polysaccharides echo the polyanionic logic of the heparin-family glycosaminoglycans (GAGs), which are known to bind chemokines and modulate leukocyte–endothelium interactions.

Charge density correlates with bioactivity. For anionic polymers, inhibition of inflammatory-cell invasion has been shown to correlate with anionic charge density — and dextran sulfate is the preferred, most active polymer class (US5605938, 1997).

A macromolecular comfort film. Strong hydrophilicity supports surface hydration, moisture retention and protective-film formation, buffering stressed skin against environmental exposure.

PUBLISHED EVIDENCE SIGNAL

−66%

reduction in neutrophil migration observed with dextran sulfate in a biological assay — direct proof that a sulfated polyanion can intervene in inflammatory-cell trafficking.

Patent FR2877565A1 — non-therapeutic use of dextran sulfate to reduce skin reactions

Neutrophil influx is an early amplifier of visible irritation and post-stress redness. Restraining this step helps keep the skin’s inflammatory response proportionate to the stress it receives.

07 · MECHANISM OVERVIEW · MECHANISM OVERVIEW

One molecule, four layers of support

Each layer is supported by published in-vitro evidence on sodium dextran sulfate or mechanistically related sulfated polysaccharides — detailed in the following sections.

08 · MECHANISM 1 — INFLAMMATORY SIGNALING · MECHANISM 1

Quietening the inflammatory microenvironment

Key experimental findings

● −42% TNF-α-induced NF-κB activation (3 mg/mL, p<0.01) — WO2020201492A1

● Strong inhibition of IL-1α and IL-8 (10 µg/mL) — Hernandez-Pigeon et al., 2018

● Reduced KLK5 and MMP-9 mRNA (stressed keratinocytes) — Hernandez-Pigeon et al., 2018

● −66% neutrophil migration — FR2877565A1

09 · EVIDENCE — SENSITIVE & ATOPIC-PRONE SKIN · THE EVIDENCE

Concentration-dependent inhibition of TSLP and IL-8

The experimental model

Normal human epidermal keratinocytes were pre-incubated with sodium dextran sulfate (MW 9–20 kDa), then stimulated for 24 hours with Poly I:C + PamC3 + IL-4 + IL-13 — mimicking an atopic inflammatory environment. TSLP and IL-8 were measured by ELISA; n = 3; p < 0.01 (vs. stimulated control).

Why it matters

● TSLP is the core alarmin released by stressed keratinocytes — it initiates the “itch–inflammation” cascade characteristic of reactive, atopic-prone skin.

● IL-8 is the key chemokine recruiting neutrophils into stressed skin.

● S-Glucan shows activity at microgram-per-milliliter concentrations — consistent with a high-potency, low-dose soothing active.

10 · MECHANISM 2 — REDNESS & VASCULAR RESPONSE · MECHANISM 2

Addressing the visible face of inflammation — redness

Visible redness is the downstream sign of the “inflammation–vascular” loop: lipid mediators dilate microvessels, while VEGF fuels vascular hyper-reactivity. In keratinocyte models of redness-prone skin, dextran sulfate acts on both arms of this loop — inflammatory mediators and the VEGF vascular axis. In a peer-reviewed study of actives for redness-prone skin (a rosacea-relevant in-vitro model), dextran sulfate was the multi-target soothing component of the system.

The model systems

● PGE2 — PMA-stimulated keratinocytes

● VEGF — LL-37 / FSL-1 / TNF-α redness environment

● Tube-like formation — VEGF-induced microvessel formation in endothelial/fibroblast co-culture

11 · MECHANISM 3 — BARRIER REPAIR · MECHANISM 3

Calmer skin recovers faster

The repair logic

Persistent low-grade inflammation keeps keratinocytes in a defensive state, blocking orderly epidermal recovery. By down-regulating alarmin and cytokine release, S-Glucan helps the epidermal environment shift from defense back to repair — supporting barrier recovery and day-after-day resilience.

Evidence boundaries

● Direct evidence: mediator inhibition in stressed keratinocytes (TSLP, IL-8, IL-1α, NF-κB).

● Mechanistic inference: barrier-repair benefit follows the “inflammation–barrier” axis described in the dermatological literature.

● Ongoing at PuriPharm: a barrier-biomarker program (filaggrin, loricrin) on the 9–20 kDa standard grade.

12 · BENEFIT ARCHITECTURE · THE BENEFITS

From mechanism to visible skin benefits

Immediate skin comfortHelps calm stressed and reactive skinHelps reduce the appearance of visible rednessHelps relieve the look and feel of irritation Sensitive skin supportDesigned for fragile, reactive skinHelps progressively improve skin toleranceSupports recovery after environmental or cosmetic stress
Barrier repairSupports epidermal recovery after stressHelps rebuild skin resilienceComplements ceramide and lipid barrier-repair systems Post-efficacy recoveryPartner active for retinoid and acid routinesHelps improve the tolerability of high-efficacy systemsSupports long-term adherence to results-driven regimens

Benefit statements are intended for cosmetic applications, anchored to the in-vitro evidence presented in the mechanism sections, and do not constitute therapeutic claims for any skin disease.

13 · DIFFERENTIATION · THE DIFFERENCE

S-Glucan vs. conventional β-glucan

Dimension Conventional β-glucan PuriActives® S-Glucan
Structural class Neutral / partially branched glucan Sulfated polyanionic polysaccharide
Backbone β-1,3 / β-1,6 glucose polymer α-1,6 dextran backbone, sulfate-esterified
Charge density Low — essentially uncharged High negative charge density (–OSO₃⁻ Na⁺)
Interaction profile Hydration, moisturizing comfort Ionic & protein interactions; inflammatory-mediator modulation
Evidence focus Hydration, comfort TSLP / IL-8 / IL-1α, NF-κB, PGE2, VEGF, neutrophil migration
Positioning Classic soothing polysaccharide Next-generation sulfated repair active

S-Glucan belongs to a distinct chemical and functional category — it should be evaluated on its own evidence base, not treated as a line extension of β-glucan.

14 · FORMULATION STRATEGY · FORMULATION STRATEGY

The tolerability partner for high-efficacy systems

The discomfort that limits retinoid, acid and vitamin C routines is inflammatory in nature — it runs through the very mediators S-Glucan down-regulates in vitro: PGE2, IL-1α, IL-8 and NF-κB. Pairing the high-efficacy engine with a repair active lets a formula preserve efficacy while improving comfort, adherence and repurchase.

Positioning principle: efficacy must be balanced with tolerability — build both into the same formulation chassis.

In the keratinocyte redness model, PGE2 was reduced by 68–70% and VEGF completely inhibited — precisely the mediator signature of active-induced irritation.

Designed to partner with

● Retinoids — retinol, retinal and their derivatives

● Exfoliating acids — AHA / BHA / PHA systems

● Vitamin C — high-strength antioxidant serums

● Dark-spot systems — tone-evening routines

● Blemish-care actives — drying, keratolytic formulas

● Post-procedure routines — after laser, peels, microneedling

S-Glucan is strongly anionic; combinations with cationic conditioning agents require formulation verification — see the Formulation Guidance section.

15 · APPLICATIONS · APPLICATIONS

Where S-Glucan delivers the most value

Anti-redness serumsTargets the PGE2 / VEGF inflammation–vascular axis behind visible redness. Daily care for sensitive skinTSLP / IL-8 modulation for daily routines for reactive and atopic-prone skin.
Post-procedure & post-laser careSupports the recovery environment after energy-based procedures and peels. Retinoid & acid recovery productsThe tolerability partner inside high-efficacy formulation chassis.
After-sun & anti-pollution careA comfort film and mediator control after environmental stress. Soothing masks & facial mistsWater-based formats are a natural fit for a readily water-soluble polyanion.
Eye contour careThin skin with visible vasculature; dextran sulfate compositions are patented for redness, puffiness and the eye contour (US6562355B1). Scalp soothing careSensitive scalp and the anti-dandruff-adjacent space — an emerging need.
After-shave careLow use levels calm mechanical-stress reactions. Minimalist gentle concepts”Skinimalist” formulas built around a single, well-characterized molecule.

Formats span serums, creams, gels, lotions, essences, masks, mists and scalp lotions — the molecule is format-agnostic in aqueous systems.

16 · FORMULATION GUIDANCE · FORMULATION GUIDANCE

Working with a strong polyanion

Simple to use

● Readily soluble in water and salt solutions — add to the water phase under conventional stirring.

● Wide pH window: reported stable in pH 4–10 solutions at room temperature, covering essentially all leave-on formats.*

● Low dose, low texture impact: effective at 0.05–0.20%; virtually no effect on viscosity or skin feel at these levels.

● Compatible with nonionic and anionic systems — conventional emulsions, gels, serums and mists.

Verify before scale-up

● Cationic ingredients: polyquaterniums, cationic surfactants and cationic conditioning polymers may form complexes with a strong polyanion — check clarity and stability.*

● Positively charged peptides — verify compatibility case by case.*

● High levels of multivalent metal ions — evaluate in the final formulation chassis.*

● Grade selection: molecular weight (9–20 vs. 4–8 kDa) and degree of sulfation both affect activity and solution behavior — fix the grade before locking the formula.

* Marked items require confirmation in the PuriPharm applications laboratory for the specific grade and formulation chassis; a full compatibility matrix is available on request.

17 · PRODUCT PROFILE · PRODUCT PROFILE

PuriActives® S-Glucan — specification summary

Product name PuriActives® S-Glucan
INCI name Sodium Dextran Sulfate
CAS No. 9011-18-1
Appearance White to off-white powder
Active content ≥ 95% (on dry basis)
Molecular weight 9–20 kDa (standard grade); 4–8 kDa grade available on request
Solubility Readily soluble in water
Recommended use level 0.05–0.20% (typical); patent literature supports 0.01–0.5%
Quality control SEC/GPC for molecular weight; elemental analysis / ICP-OES for sulfur content; ion chromatography for free sulfate — documented per batch on the CoA
Microbiology & heavy metals Controlled to cosmetic ingredient standards

The degree of sulfation is defined per grade and documented batch-by-batch on the Certificate of Analysis (CoA), rather than stated as a single generic value — see the Quality & Analytics section.

18 · QUALITY & ANALYTICS · QUALITY & ANALYTICS

Not all sodium dextran sulfate is equal

Sodium dextran sulfate is a distribution-defined polymer: even with identical INCI and CAS, differences in molecular weight, molecular-weight distribution, degree of sulfation and free-sulfate residue all change protein binding, ionic strength, viscosity and bioactivity. S-Glucan is therefore defined by a dual-axis specification — molecular weight × degree of sulfation — never by INCI alone.

Batch-level analytical control

● SEC / GPC — Mw, Mn and polydispersity for every batch

● Elemental analysis / ICP-OES — total sulfur content

● Ion chromatography — free sulfate residue

● ¹H / ¹³C NMR — backbone and sulfation-site confirmation

● FTIR — characteristic S=O and C–O–S bands

● Moisture, ash, sodium content, conductivity — batch-to-batch consistency

Defined structure → defined performance: every batch of S-Glucan ships with the complete analytical fingerprint a formulator needs to reproduce results.

19 · KEY TAKEAWAYS · KEY TAKEAWAYS

Why formulators choose S-Glucan

01 A category of its own, not another glucan. Sulfation converts a neutral polysaccharide into a strong polyanionic repair active with a fundamentally different interaction profile.

02 A multi-target, literature-backed mechanism. Concentration-dependent inhibition of TSLP and IL-8; inhibition of IL-1α, KLK5 and MMP-9; reduced NF-κB activation; up to 66% less neutrophil migration.

03 Active on both arms of the redness loop. In published keratinocyte and co-culture models: PGE2 reduced by 68–70%, VEGF completely inhibited, and VEGF-driven microvessel formation reduced by 47–54%.

04 The tolerability partner modern formulas need. Purpose-built for sensitive skin, post-procedure care and high-efficacy retinoid/acid systems — at use levels of just 0.05–0.20%.

05 Defined by science, not traded as a commodity. A dual-axis molecular weight × sulfation specification with full batch analytics from PuriPharm — reproducible performance, batch after batch.

20 · REFERENCES · REFERENCES

Sources and scientific basis

Peer-reviewed literature

1. Hernandez-Pigeon H, Garidou L, Galliano M-F, et al. Effects of dextran sulfate, 4-t-butylcyclohexanol, pongamia oil and hesperidin methyl chalcone on inflammatory and vascular responses implicated in rosacea. Clin Cosmet Investig Dermatol. 2018;11:405–414. doi:10.2147/CCID.S168621

2. Misery L, Sibaud V, Merial-Kieny C, Taieb C. Sensitive skin in the American population: prevalence, clinical data, and role of the dermatologist. Int J Dermatol. 2011;50(8):961–967.

3. Farage MA. The prevalence of sensitive skin. Cosmetics. 2019;6(2):26.

Patent literature

4. WO2020201492A1 / CN113766922A — dextran sulfate and compositions thereof for inflammatory skin conditions; TSLP / IL-8 / NF-κB experimental data, 2020.

5. FR2877565A1 — non-therapeutic use of dextran sulfate for preventing and/or reducing skin reactions; neutrophil migration experimental data, priority 2004.

6. US6562355B1 — dextran sulfate / escin compositions for skin redness, puffiness and sensitive skin, including eye contour care, 2003.

7. US5605938 — anionic polymers inhibiting cell invasion; activity correlated with anionic charge density, 1997.

Market data

8. Mordor Intelligence. Dermocosmetics Skin Care Products Market — Size, Share & Forecasts (2026–2031). 2026 edition.

9. Future Market Insights. Repairing Skin Care Treatments Market Forecast and Outlook 2026 to 2036. 2026.

The in-vitro data cited in the mechanism sections originate from sodium dextran sulfate of the same INCI category as PuriActives® S-Glucan; the data characterize the technology platform, were redrawn from the cited sources, and the values were not altered.

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